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2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE

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2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Basic information

Product Name:
2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE
Synonyms:
  • 2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE
  • 2,4-DIAMINO-5-PYRIMIDINECARBONITRILE
  • 2,4-DIAMINO-5-CYANO-PYRIMIDINE
  • 5-Pyrimidinecarbonitrile, 2,4-diamino- (6CI,8CI,9CI)
  • 2,4-Diaminopyrimidine-5-carbonitrile ,97%
  • NSC 135235
  • 2,4-Diaminopyrimidine-5-carbonitriL
  • 5-Pyrimidinecarbonitrile, 2,4-diamino-
CAS:
16462-27-4
MF:
C5H5N5
MW:
135.13
Product Categories:
  • Heterocycle-Pyrimidine series
  • Amines
  • Aromatics
  • Heterocycles
  • Intermediates
  • PYRIMIDINE
Mol File:
16462-27-4.mol
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2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Chemical Properties

Melting point:
318 °C (decomp)
Boiling point:
498.2±55.0 °C(Predicted)
Density 
1.45±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,2-8°C
solubility 
DMF (Slightly, Heated), DMSO (Slightly)
form 
Solid
pka
3.93±0.10(Predicted)
color 
Light Yellow
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Safety Information

HS Code 
29335990
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2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Usage And Synthesis

Chemical Properties

Yellow Solid

Uses

2,4-Diaminopyrimidine-5-carbonitrile is used as an intermediate for the preparation of medicines and agrochemicals (1).

Uses

Intermediate for the preparation of medicines and agrochemicals.

Synthesis

506-93-4

123-06-8

16462-27-4

General procedure for the synthesis of 2,4-diaminopyrimidine-5-carbonitrile from guanidine nitrate and ethoxymethylenemalonononitrile: 1.22 g (10 mmol) of guanidine nitrate was dissolved in 50 mL of sodium ethanolate ethanol solution, keeping the reaction temperature at 5°C, and 1.22 g (10 mmol) of ethoxymethylenemalononitrile was added slowly dropwise, the dropwise process lasted for 8 hours. Upon completion of the reaction, the reaction was quenched by the addition of an appropriate amount of water and extracted with ethyl acetate. The organic phases were combined and washed with saturated saline, followed by concentration of the organic phase by removing the solvent by distillation under reduced pressure. Finally, the residue was purified by silica gel column chromatography with an eluent ratio of dichloromethane:methanol=1:30 (v/v) to afford the white solid product 2,4-diaminopyrimidine-5-carbonitrile (compound of formula IV) in 71% yield.

References

[1] Patent: CN106938997, 2017, A. Location in patent: Paragraph 0048; 0058-0059
[2] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 9, p. 3187 - 3197

2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Preparation Products And Raw materials

Raw materials

2,4-DIAMINOPYRIMIDINE-5-CARBONITRILESupplier

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